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Results: 1-9 |
Results: 9
Maternal component in the familial aggregation of hypertension
Authors: DeStefano, AL Gavras, H Heard-Costa, N Bursztyn, M Manolis, A Farrer, LA Baldwin, CT Gavras, I Schwartz, F
Citation: Al. Destefano et al., Maternal component in the familial aggregation of hypertension, CLIN GENET, 60(1), 2001, pp. 13-21
Otopathology in a case of type I Waardenburg's syndrome
Authors: Merchant, SN McKenna, MJ Baldwin, CT Milunsky, A Nadol, JB
Citation: Sn. Merchant et al., Otopathology in a case of type I Waardenburg's syndrome, ANN OTOL RH, 110(9), 2001, pp. 875-882
Genetic predisposition to stroke in relatives of hypertensives
Authors: Nicolaou, M DeStefano, AL Gavras, I Cupples, LA Manolis, AJ Baldwin, CT Gavras, H Farrer, LA
Citation: M. Nicolaou et al., Genetic predisposition to stroke in relatives of hypertensives, STROKE, 31(2), 2000, pp. 487-492
Identification of a polymorphic glutamic acid stretch in the alpha(2B)-adrenergic receptor and lack of linkage with essential hypertension
Authors: Baldwin, CT Schwartz, F Baima, J Burzstyn, H DeStefano, AL Gavras, I Handy, DE Joost, O Martel, T Manolis, A Nicolaou, M Bresnahan, M Farrer, L Gavras, H
Citation: Ct. Baldwin et al., Identification of a polymorphic glutamic acid stretch in the alpha(2B)-adrenergic receptor and lack of linkage with essential hypertension, AM J HYPERT, 12(9), 1999, pp. 853-857
Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease
Authors: Joost, O Taylor, CA Thomas, CA Cupples, LA Saint-Hilaire, MH Feldman, RG Baldwin, CT Myers, RH
Citation: O. Joost et al., Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease, MOVEMENT D, 14(4), 1999, pp. 590-595
Bioturbation in an active deep-sea area: Implications for models of trace fossil tiering
Authors: Baldwin, CT McCave, IN
Citation: Ct. Baldwin et In. Mccave, Bioturbation in an active deep-sea area: Implications for models of trace fossil tiering, PALAIOS, 14(4), 1999, pp. 375-388
Evidence for linkage between essential hypertension and a putative locus on human chromosome 17
Authors: Baima, J Nicolaou, M Schwartz, F DeStefano, AL Manolis, A Gavras, I Laffer, C Elijovich, F Farrer, L Baldwin, CT Gavras, H
Citation: J. Baima et al., Evidence for linkage between essential hypertension and a putative locus on human chromosome 17, HYPERTENSIO, 34(1), 1999, pp. 4-7
Mitochondrial DNA mutations in patients with orthostatic hypotension
Authors: Schwartz, F Baldwin, CT Baima, J Gavras, H
Citation: F. Schwartz et al., Mitochondrial DNA mutations in patients with orthostatic hypotension, AM J MED G, 86(2), 1999, pp. 145-150
A locus for autosomal recessive achromatopsia on human chromosome 8q
Authors: Milunsky, A Huang, XL Milunsky, J DeStefano, A Baldwin, CT
Citation: A. Milunsky et al., A locus for autosomal recessive achromatopsia on human chromosome 8q, CLIN GENET, 56(1), 1999, pp. 82-85
Risultati: 1-9 |